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白细胞介素-10根据人单核细胞白血病细胞系UG3中的环境不同地调节单核细胞趋化蛋白-1基因的表达。

Interleukin-10 differently regulates monocyte chemoattractant protein-1 gene expression depending on the environment in a human monoblastic cell line, UG3.

作者信息

Ikeda Takashi, Sato Ken, Kuwada Naruo, Matsumura Takuya, Yamashita Takuya, Kimura Fumihiko, Hatake Kiyohiko, Ikeda Kazuma, Motoyoshi Kazuo

机构信息

Third Department of Internal Medicine, National Defense Medical College, Saitama, Japan.

出版信息

J Leukoc Biol. 2002 Dec;72(6):1198-205.

Abstract

Interleukin (IL)-4, IL-10, and IL-13 affect monocyte/macrophage functions including regulation of cytokine production. We analyzed the regulatory effects of these cytokines on cytokine production using a human monoblastic cell line, UG3. It is interesting that IL-10 up-regulated, whereas IL-4 and IL-13 down-regulated monocyte chemoattractant protein-1 (MCP-1) production by unstimulated UG3 cells. IL-10-induced expression of MCP-1 mRNA occurred without de novo protein synthesis at transcriptional and post-transcriptional levels. The enhancement of binding activity of nuclear factor Sp1 (Sp-1) and signal transducer and activators of transcription (STAT)1 and 3 but not nuclear factor kappaB (NF-kappaB) was associated with this IL-10-induced MCP-1 expression. Furthermore, IL-10 suppressed lipopolysaccharide (LPS)-induced NF-kappaB binding but not Sp-1. The present results suggest IL-10 has two contrasting actions on the MCP-1 production of monocytes/macrophages, between the resting and activated conditions. The combination of activated Sp-1 and STATs is important for IL-10-induced MCP-1 expression in resting monocytes/macrophages, and the inhibition of LPS-induced NF-kappaB binding is crucial for down-regulation of MCP-1 by IL-10 in stimulated monocytes/macrophages.

摘要

白细胞介素(IL)-4、IL-10和IL-13影响单核细胞/巨噬细胞功能,包括细胞因子产生的调节。我们使用人单核母细胞系UG3分析了这些细胞因子对细胞因子产生的调节作用。有趣的是,IL-10上调未受刺激的UG3细胞单核细胞趋化蛋白-1(MCP-1)的产生,而IL-4和IL-13下调其产生。IL-10诱导的MCP-1 mRNA表达在转录和转录后水平均无需从头合成蛋白质即可发生。核因子Sp1(Sp-1)、信号转导子和转录激活子(STAT)1和3而非核因子κB(NF-κB)结合活性的增强与这种IL-10诱导的MCP-1表达相关。此外,IL-10抑制脂多糖(LPS)诱导的NF-κB结合,但不抑制Sp-1。目前的结果表明,IL-10在静息和激活状态下对单核细胞/巨噬细胞的MCP-1产生有两种相反的作用。激活的Sp-1和STATs的组合对于IL-10诱导静息单核细胞/巨噬细胞中MCP-1的表达很重要,而抑制LPS诱导的NF-κB结合对于IL-10下调受刺激单核细胞/巨噬细胞中MCP-1至关重要。

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